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American Journal of Diseases of Children (1960)|September 1, 1987
Lack of effect of lithium carbonate in patients with glycogenosis IbD H Mahoney, D R Ambruso, E R McCabe, et al.Biochemical Medicine and Metabolic Biology|August 1, 1991
Screening for cystic fibrosis: feasibility of molecular genetic analysis of dried blood specimensW K Seltzer, F Accurso, M Z Fall, et al.The Journal of Clinical Investigation|April 1, 1988
Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphataseM P Whyte, J D Mahuren, K N Fedde, et al.Genomics|July 1, 1990
DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysisJ A Towbin, J S Chamberlain, D R Wu, et al.Lancet (London, England)|August 31, 1991
Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cardsY Matsubara, K Narisawa, K Tada, et al.Molecular Genetics and Metabolism|January 4, 2001
Midkine is expressed early in rat fetal adrenal developmentP Dewing, S T Ching, Y H Zhang, et al.The Journal of Pediatrics|October 1, 1978
Homotransplantation of the liver in a patient with hepatoma and hereditary tyrosinemiaR O Fisch, E R McCabe, D Doeden, et al.European Journal of Pediatrics|November 1, 1987
Infantile glycerol kinase deficiency--a condition requiring prompt identification. Clinical, biochemical, and morphological findings in two casesA Kohlschütter, H P Willig, D Schlamp, et al.Journal of Inherited Metabolic Disease|January 1, 1989
The management of breast feeding among infants with phenylketonuriaL McCabe, A E Ernest, M R Neifert, et al.American Journal of Human Genetics|November 1, 1990
Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophyD A Pillers, J A Towbin, J S Chamberlain, et al.Pageof 12